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Cordis Ducor Ptr System

by Cordis Corp.

510(k) K811971

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK811971 Date13 Aug 1981ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
DQY
Device class
Class II
Regulation
21 CFR Part 870.1250
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

Overview

AI-generated summary, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Cordis Ducor Ptr System is a percutaneous transluminal recanalization system designed to facilitate the placement of venous stents, providing a pathway for stent delivery in obstructed or narrowed veins and aiding in the restoration of normal blood flow. It is classified as a Catheter, Percutaneous, and is used in the Cardiovascular medical specialty.

The system is supplied with a product code of DQY and has been assigned the FDA 510(k) clearance number K811971, with a decision description of Substantially Equivalent. The device was reviewed by the Cardiovascular advisory committee and has a clearance type of Traditional, with a decision date of August 13, 1981.

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Questions

AI-generated answers, 22 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the Cordis Ducor Ptr System used for?

    The Cordis Ducor Ptr System is used to facilitate the placement of venous stents, providing a pathway for stent delivery in obstructed or narrowed veins and aiding in the restoration of normal blood flow.

  • What type of device is the Cordis Ducor Ptr System?

    The Cordis Ducor Ptr System is classified as a Catheter, Percutaneous, and is used in the Cardiovascular medical specialty.

  • What is the product code for the Cordis Ducor Ptr System?

    The Cordis Ducor Ptr System has been assigned the product code DQY.

  • What is the regulatory status of the Cordis Ducor Ptr System?

    The Cordis Ducor Ptr System has been assigned the FDA 510(k) clearance number K811971, with a decision description of Substantially Equivalent.